METHOD FOR PRODUCING (1R,2S,5S)-N-[(1S)-1-CYANO-2-[(3S)-2-OXOPYRRROLIDIN-3-YL]ETHYL]-3-[(2S)-3,3- DIMETHYL-2-[(2,2,2-TRIFLUORACETYL)AMINO]BUTANOYL]-6,6-DIMETHYL-3-AZABICYCLO[3.1.0]HEXAN-2-CARBOXAMIDE Russian patent published in 2023 - IPC C07D209/52 C07D403/12 A61K31/403 

Abstract RU 2794755 C1

FIELD: medicine; pharmacology; pharmaceutical industry.

SUBSTANCE: group of inventions includes a method for producing (1R,2S,5S)-N-[(1S)-1-cyano-2-[(3S)-2-oxopyrrolidin-3-yl]ethyl]-3-[(2S)-3,3-dimethyl-2-[(2,2,2-trifluoroacetyl)amino]butanoyl]-6,6-dimethyl-3-azabicyclo[3.1.0]hexane- 2-carboxamide (compound of formula (I)) and its use for batch chemical industrial production, semi-continuous industrial production or continuous industrial production, as well as a method for preparing an intermediate compound of formula (IV) intended for use in a method for producing a compound of formula (I). The process for preparing a compound of formula (I) includes the following steps: a) reaction of a compound of formula (V) or a salt thereof with a compound of formula (IV) using a compound of formula RO-CO-Cl, where R is C1-C5 alkyl; C1-C5 alkyl substituted with halogen; phenyl; phenyl substituted with halogen, nitro, C1-C5 alkyl, or benzyl substituted with halogen, nitro, C1-C5 alkyl, in the presence of a base to give a compound of formula (VI); b) dehydration of the compound of formula (VI) using 2,4,6-trichloro-1,3,5-triazine to form a compound of formula (I). In this case, the method for obtaining an intermediate compound of formula (IV) includes the interaction of a compound of formula (II) with a compound of formula (III) or its salts in an organic solvent in the presence of a base , provided that R1 is selected from pentafluorophenyl and succinimidyl, R2 is hydrogen; when R1 is hydrogen, R2 is t-butyl, the reaction is carried out in the presence of a compound of the formula RO-CO-Cl, where R is C1-C5 alkyl; C1-C5 alkyl substituted with halogen; phenyl; phenyl substituted with halogen, nitro, C1-C5 alkyl, or benzyl substituted with halogen, nitro, C1-C5 alkyl.

EFFECT: improved method of obtaining, leading to an increase in the yield and chemical purity of the compound of formula (I).

48 cl, 1 tbl, 2 ex

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RU 2 794 755 C1

Authors

Belyj Petr Aleksandrovich

Lopatukhin Eduard Yurevich

Korolev Vladimir Lvovich

Zaslavskaya Kira Yakovlevna

Belov Evgenij Yurevich

Dates

2023-04-24Published

2022-04-15Filed